Have questions? Visit https://www.reddit.com/r/SNPedia

rs484959

From SNPedia

Orientationminus
Stabilizedminus
Make rs484959(A;A)
Make rs484959(A;G)
Make rs484959(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position109823461
is asnp
is mentioned by
dbSNPrs484959
ebirs484959
HLIrs484959
Exacrs484959
Varsomers484959
Maprs484959
PheGenIrs484959
hapmaprs484959
1000 genomesrs484959
hgdprs484959
ensemblrs484959
gopubmedrs484959
geneviewrs484959
scholarrs484959
googlers484959
pharmgkbrs484959
gwascentralrs484959
openSNPrs484959
23andMers484959
23andMe allrs484959
SNP Nexus

SNPshotrs484959
SNPdbers484959
MSV3drs484959
GWAS Ctlgrs484959
GMAF0.4991
Max Magnitude
? (A;A) (A;G) (G;G) 28
related to Paget’s disease of bone 23andMe blog.
GWAS snp
PMID [PMID 20436471OA-icon.png]
Trait Paget's disease
Title Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
Risk Allele
P-val 5E-24
Odds Ratio 1.82 [1.61-2.04]
OMIM602080
Desc
Variant
Relatedalso